Canonical Allele Identifier: CA2270103104

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832495T= , CM000679.2:g.63832495T=	GRCh38
NC_000017.10:g.61909855T= , CM000679.1:g.61909855T=	GRCh37
NC_000017.9:g.59263587T=	NCBI36
NG_053004.1:g.15497A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2318A=
ENST00000697953.1:n.2891A=
ENST00000698013.1:n.3003A=
ENST00000698014.1:n.3226A=
ENST00000698015.1:n.2319A=
ENST00000698016.1:c.*443A=	ENSP00000513502.1:n.*443A=
ENST00000698017.1:n.2393A=
ENST00000698018.1:n.2524A=
ENST00000698019.1:n.2722A=
ENST00000698020.1:n.1828A=
ENST00000698021.1:c.1737A=
ENST00000698022.1:c.*443A=	ENSP00000513504.1:n.*443A=
ENST00000698023.1:n.2422A=
ENST00000698024.1:n.2284A=
ENST00000698025.1:n.2444A=
ENST00000698026.1:n.1335A=
ENST00000698027.1:c.*660A=	ENSP00000513505.1:n.*660A=
ENST00000698028.1:n.2527A=
ENST00000698029.1:n.3256A=
ENST00000448276.7:c.*443A= MANE Select	ENSP00000392617.2:n.*443A=
ENST00000448276.6:c.*443A=	ENSP00000392617.2:n.*443A=
ENST00000613943.4:c.1928A=	ENSP00000483605.1:n.1928A=
NM_001098426.1:c.*443A=	NP_001091896.1:n.*443A=
XM_005257604.2:c.*443A=	XP_005257661.2:n.*443A=
NM_001330439.1:c.*443A=	NP_001317368.1:n.*443A=
NM_001330440.1:c.*443A=	NP_001317369.1:n.*443A=
NM_001098426.2:c.*443A= MANE Select	NP_001091896.1:n.*443A=
NM_001330440.2:c.*443A=	NP_001317369.1:n.*443A=